• Bulletin of the Korean Chemical Society
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• v.23 no.1
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• pp.103-106
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• 2002

A new reaction mechanism is proposed for the reaction of thianthrene cation radical perchlorate $(Th^{+{\cdot}}CIO_4^-}$ and tert-butyl peroxide in acetonitrile at room temperature on the basis of experimental and theoretical results. Rapid C-O bond rupture instead of O-O bond cleavage was observed by a good peroxy radical trapping agent, thianthrene cation radical. Products were N-tert-butyl acetamide, thianthrene 5-oxide (ThO), thianthrene 5,5-dioxide $(SSO_2)$, and thianthrene (Th). Thianthrene 5,10-dioxide (SOSO) was not obtained. A comparative computational study of the cation radical of tert-butyl peroxide is made by using B3LYP and CBS-4. The computational results are helpful to explain the reaction mechanism.

• Journal of the Korean Institute of Illuminating and Electrical Installation Engineers
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• v.27 no.7
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• pp.45-51
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• 2013

This study is to discuss simulation results with 51 principal chemical reactions in non-thermal plasma space under atmospheric pressure, and the ambient gas was mainly composed of oxygen and nitrogen molecules. The initial density of O and OH radicals under the ambient temperature of 300K is largely generated in comparison with other higher temperature, and the density of O radical decreased from $20{\mu}s$ according to increase the temperature. The initial density of OH radical seemed to decrease steeply at the initial stage. By increasing the initial density of $H_2O$ molecules, O radical's effect was few and the density of OH radical was largely generated about 2 times. In addition, ozone density was increased as increasing the density of O radical, but it was decreased as increasing the density of $H_2O$. In case of the temperature more than 300K, $NO_2$ tend to be removed, but NO was increased than the initial density.

• Journal of Korean Society on Water Environment
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• v.28 no.2
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• pp.219-223
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• 2012

The fixed solid catalysts such as glass bead, steel mesh, and $TiO_2$ coated ceramic bead were used to investigate effect of radical production at different frequencies. The radical production rate at 300 kHz was faster than that at 35 kHz without solid, but the tendency was changed with the presence of glass bead. The presence of glass beads create non-continuous points between the solid and liquid phases leading to increased formation of cavitation bubbles. However, the radical production decreased when steel mesh was used at 35 kHz although the surface area of contact with liquid was same when glass bead was used. Hence the solid catalyst did not always enhance the radical production. The radical production using $TiO_2$ coated ceramic bead was dramatically increased at 35 kHz due to the breakage of $TiO_2$ coated ceramic bead. Therefore the radical productions at 300 kHz using fixed solid catalysts generally increased while at 35 kHz the results fluctuated according to the experimental conditions.

• Journal of Environmental Science International
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• v.20 no.7
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• pp.891-898
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• 2011

The aim of this research was to evaluate the effect of combination of disinfection process (electrolysis, UV process) on Escherichia coli (E. coli) disinfection and oxidants (OH radical, $ClO_2$, HOCl, $H_2O_2$ and $O_3$) generation. The effect of electrolyte type (NaCl, KCl and $Na_2SO_4$) on the E. coli disinfection and oxidants generation were evaluated. The experimental results showed that performance of E. coli disinfection of electrolysis and UV single process was similar. Combination of electrolysis and UV process enhanced the E. coli disinfection and 4-carboxybenzaldehyde (4-CBA, indicator of the generation of OH radical) degradation. It is clearly showed synergy effect on disinfection and OH radical formation. However chlorine ($ClO_2$, HOCl) and oxygen type ($H_2O_2$, $O_3$) oxidants were decreased with the combination of two process. In electrolysis + UV complex process, electro-generated $H_2O_2$ and $O_3$ were reacted with UV light of UV-C lamp and increased 4-CBA degradation(increase OH radical). Disinfection of electrolyte of chlorine type was higher than that of the sulfate type electrolyte due to the higher generation of OH radical and oxidants.

• BMB Reports
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• v.43 no.3
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• pp.219-224
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• 2010

Lipid peroxidation is known to be an important factor in the pathologies of many diseases associated with oxidative stress. We assessed the lipid peroxidation induced by the reaction of ferritin with $H_2O_2$. When linoleic acid micelles or phosphatidyl choline liposomes were incubated with ferritin and $H_2O_2$, lipid peroxidation increased in the presence of ferritin and $H_2O_2$ in a concentration-dependent manner. The hydroxyl radical scavengers, azide and thiourea, prevented lipid peroxidation induced by the ferritin/$H_2O_2$ system. The iron specific chelator desferoxamine also prevented ferritin/$H_2O_2$ systemmediated lipid peroxidation. These results demonstrate the possible role of iron in ferritin/$H_2O_2$ system-mediated lipid peroxidation. Carnosine is involved in many cellular defense processes, including free radical detoxification. In this study, carnosine, homocarnosine, and anserine were shown to significantly prevent ferritin/$H_2O_2$ system-mediated lipid peroxidation and also inhibited the free radical-generation activity of ferritin. These results indicated that carnosine and related compounds may prevent ferritin/$H_2O_2$ system-mediated lipid peroxidation via free radical scavenging.

• Journal of Adhesion and Interface
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• v.2 no.2
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• pp.11-19
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• 2001

The phase-transfer catalyzed radical polymerization of styrene was carried out using tricaprylylmethylammonium chloride as a phase-transfer catalyst in a two-phase system of an aqueous $Na_2S_2O_8$ solution and toluene at $60^{\circ}C$ under nitrogen atmosphere. The initial rate of radical polymerization was expressed as the combined terms of concentrations of quaternary onium cation and peroxydisulfate anion in the aqueous phase rather than the fed concentrations of catalyst and $Na_2S_2O_8$. The observed initial rate of radical polymerization was used to analyze the radical polymerization mechanism with a cycle phase-transfer initiation step in the heterogeneous liquid-liquid system. The viscosity average molecular weight of polystyrene was inversely proportional to concentration of $Na_2S_2O_8$ expressed as $[Q^+]([S_2O{_8}^{2-}]{\alpha}_2)^{1/2}$ derived by the radical polymerization mechanism.

• Herbal Formula Science
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• v.12 no.1
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• pp.255-262
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• 2004

The inhibitory effect of the aerial parts of Fagopyrum esculentum on the 1,1-diphenyl-2-picrylhydrazyl (DPPH) radical was examined. The n-butanol fraction from the methanol extract of title plant showed stronger inhibitory effect than other fractions on DPPH radical. Two flavonoids were isolated from n-butanol fraction having the potent activity and elucidated as quercetin-3-O-${\alpha}$-L-rhamnoside and quercetin-3-O-rutinoside on the basis of spectral evidence. The $IC_{50}$ values of these compounds on DPPH radical were 6.56 ${\mu}M$ and 8.37 ${\mu}M$, respectively.

• Bulletin of the Korean Chemical Society
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• v.16 no.3
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• pp.281-284
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• 1995

The visible emission spectra of the o-xylyl radical in the gas phase have been obtained using a Fourier transform spectrometer coupled with a technique of supersonic expansion. The o-xylyl radical was generated in a jet by expansion with an inert buffer gas He from a high voltage dc discharge of the precursor o-xylene. The spectra were analyzed on the basis of the rotational contours of the vibronic bands as well as the known vibrational frequencies by a matrix isolation method.

• Journal of Korean Society on Water Environment
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• v.35 no.6
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• pp.550-556
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• 2019

This study was carried out to improve the photocatalytic reaction of TiO₂ photocatalyst. During the photocatalytic reaction, OH radicals are generated and they have an excellent oxidation capability for wastewater treatment. To evaluate the OH radicals generated according to crystallographic structure of TiO₂ nanotubes photocatalyst, a probe compound, 4-Chlorobenzoic acid was monitored to evaluate OH radical. Ultraviolet light was applied for photocatalytic reaction of TiO₂. The 4-Chlorobenzoic acid solution was prepared at laboratory. TiO₂ nanotube was grown on titanium plate by using anodization method. The annealing temperature for TiO₂ nanotube was varied from 400 to 900 ℃ and the crystal forms of the TiO₂ nanotube was analyzed. Depending on annealing temperature, TiO₂ nanotubes have shown different crystal forms; 100% anatase (0 % rutile), 18.4 % rutile (81.6 % anatase), 36.6 % rutile (63.4 % anatase) and 98.6% rutile (1.4% anatase). As the annealing temperature increases, the rutile ratio increases. OH radical generation from 18.4 % rutile TiO₂ nanotube plate was about 3.8 times higher than before annealing and 1.4 times higher than only 100 % anatase-TiO₂ nanotube. The efficiency of the 18.4% rutile TiO₂ nanotube was the best in comparison to TiO₂ nanotube with 18.4 %, 36.6 % and 98.6 % rutile. As a result, photocatalytic ability of 18.4 % rutile-TiO₂ nanotube plate was higher than 100 % anatase-TiO₂ nanotube plate.

• Journal of Korean Society on Water Environment
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• v.32 no.5
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• pp.403-409
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• 2016

In this study, a TiO₂ nanotube was grown on a titanium plate by using anodic oxidation method for the evaluation of TiO₂ nanotube morphology. The TiO₂ nanotube was grown in an electrolyte containing ethylene glycol, 0.2 wt% of NH₄F and 2 vol% of H₂O. Applied voltage varied from 30 to 70 V and the morphology of the TiO₂ nanotube was observed. After anodization, a TiO₂ nanotube plate was immersed in 35℃ ethanol for 24 hours. Anatase and rutile crystal forms of TiO₂ nanoutbe were observed after annealing. 4-chrolobenzoic acid, a probe compound for OH radicals, was dissolved in H₂O in order to measure the OH radical. Liquid chromatography was used to check the concentration of the 4-chrolobenzoic acid. The OH radical generation by TiO₂ nanotube plate was proportionate to the length of the TiO₂ nanotube. Furthermore, when the number of TiO₂ nanotube plate increased, the OH radical generation increased as well.